Literature DB >> 22566169

Hereditary autoinflammatory syndromes: a Brazilian multicenter study.

Adriana A Jesus1, Erika Fujihira, Mariana Watase, Maria T Terreri, Maria O Hilario, Magda Carneiro-Sampaio, Claudio A Len, Sheila K Oliveira, Marta C Rodrigues, Rosa M Pereira, Blanca Bica, Nilzio A Silva, Andre Cavalcanti, Roberto Marini, Flavio Sztajnbok, Maria V Quintero, Virginia P Ferriani, Dewton Moraes-Vasconcelos, Clovis A Silva, Joao B Oliveira.   

Abstract

OBJECTIVE: To evaluate the prevalence of genetic defects in clinically suspected autoinflammatory syndromes (AIS) in a Brazilian multicenter study.
METHODS: The study included 102 patients with a clinical diagnosis of Cryopyrin Associated Periodic Syndromes (CAPS), TNF Receptor Associated Periodic Syndrome (TRAPS), Familial Mediterranean Fever (FMF), Mevalonate Kinase Deficiency (MKD) and Pediatric Granulomatous Arthritis (PGA). One of the five AIS-related genes (NLRP3, TNFRSF1A, MEFV, MVK and NOD2) was evaluated in each patient by direct DNA sequencing, based on the most probable clinical suspect.
RESULTS: Clinical diagnoses of the 102 patients were: CAPS (n = 28), TRAPS (n = 31), FMF (n = 17), MKD (n = 17) and PGA (n = 9). Of them, 27/102 (26 %) had a confirmed genetic diagnosis: 6/28 (21 %) CAPS patients, 7/31 (23 %) TRAPS, 3/17 (18 %) FMF, 3/17 (18 %) MKD and 8/9 (89 %) PGA.
CONCLUSION: We have found that approximately one third of the Brazilian patients with a clinical suspicion of AIS have a confirmed genetic diagnosis.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22566169     DOI: 10.1007/s10875-012-9688-x

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  44 in total

1.  dbSNP: the NCBI database of genetic variation.

Authors:  S T Sherry; M H Ward; M Kholodov; J Baker; L Phan; E M Smigielski; K Sirotkin
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

2.  Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.

Authors:  M F McDermott; I Aksentijevich; J Galon; E M McDermott; B W Ogunkolade; M Centola; E Mansfield; M Gadina; L Karenko; T Pettersson; J McCarthy; D M Frucht; M Aringer; Y Torosyan; A M Teppo; M Wilson; H M Karaarslan; Y Wan; I Todd; G Wood; R Schlimgen; T R Kumarajeewa; S M Cooper; J P Vella; C I Amos; J Mulley; K A Quane; M G Molloy; A Ranki; R J Powell; G A Hitman; J J O'Shea; D L Kastner
Journal:  Cell       Date:  1999-04-02       Impact factor: 41.582

3.  NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain.

Authors:  Carlos D Rosé; Juan I Aróstegui; Tammy M Martin; Graciela Espada; Lisabeth Scalzi; Jordi Yagüe; James T Rosenbaum; Consuelo Modesto; Maria Cristina Arnal; Rosa Merino; Julia García-Consuegra; María Antonia Carballo Silva; Carine H Wouters
Journal:  Arthritis Rheum       Date:  2009-06

4.  Common MEFV mutation analysis in 36 Iranian patients with familial Mediterranean fever: clinical and demographic significance.

Authors:  Ali Bidari; Banafsheh Ghavidel-Parsa; Hossein Najmabadi; Elham Talachian; Majid Haghighat-Shoar; Behrooz Broumand; Babak Ghalehbaghi
Journal:  Mod Rheumatol       Date:  2010-06-15       Impact factor: 3.023

5.  Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium.

Authors: 
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

6.  A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients.

Authors:  L Federici; C Rittore-Domingo; I Koné-Paut; C Jorgensen; M Rodière; A Le Quellec; I Touitou
Journal:  Ann Rheum Dis       Date:  2006-05-17       Impact factor: 19.103

7.  Differentiating PFAPA syndrome from monogenic periodic fevers.

Authors:  Marco Gattorno; Roberta Caorsi; Antonella Meini; Marco Cattalini; Silvia Federici; Francesco Zulian; Elisabetta Cortis; Giuseppina Calcagno; Alberto Tommasini; Rita Consolini; Gabriele Simonini; Maria Antonietta Pelagatti; Maurizia Baldi; Isabella Ceccherini; Alessandro Plebani; Joost Frenkel; Maria Pia Sormani; Alberto Martini
Journal:  Pediatrics       Date:  2009-09-28       Impact factor: 7.124

8.  Familial Mediterranean fever gene mutations in the inner northern region of Turkey and genotype-phenotype correlation in children.

Authors:  Resul Yilmaz; Samet Ozer; Huseyin Ozyurt; Unal Erkorkmaz; Semsettin Sahin
Journal:  J Paediatr Child Health       Date:  2009-10-19       Impact factor: 1.954

9.  Long-term follow-up, clinical features, and quality of life in a series of 103 patients with hyperimmunoglobulinemia D syndrome.

Authors:  Jeroen C H van der Hilst; Evelien J Bodar; Karyl S Barron; Joost Frenkel; Joost P H Drenth; Jos W M van der Meer; Anna Simon
Journal:  Medicine (Baltimore)       Date:  2008-11       Impact factor: 1.889

10.  Infevers: an evolving mutation database for auto-inflammatory syndromes.

Authors:  Isabelle Touitou; Suzanne Lesage; Michael McDermott; Laurence Cuisset; Hal Hoffman; Catherine Dode; Nitza Shoham; Ebun Aganna; Jean-Pierre Hugot; Carol Wise; Hans Waterham; Denis Pugnere; Jacques Demaille; Cyril Sarrauste de Menthiere
Journal:  Hum Mutat       Date:  2004-09       Impact factor: 4.878

View more
  11 in total

Review 1.  Familial Mediterranean fever: An updated review.

Authors:  İsmail Sarı; Merih Birlik; Timuçin Kasifoğlu
Journal:  Eur J Rheumatol       Date:  2014-03-01

2.  The 2021 EULAR/American College of Rheumatology Points to Consider for Diagnosis, Management and Monitoring of the Interleukin-1 Mediated Autoinflammatory Diseases: Cryopyrin-Associated Periodic Syndromes, Tumour Necrosis Factor Receptor-Associated Periodic Syndrome, Mevalonate Kinase Deficiency, and Deficiency of the Interleukin-1 Receptor Antagonist.

Authors:  Micol Romano; Z Serap Arici; David Piskin; Sara Alehashemi; Daniel Aletaha; Karyl Barron; Susanne Benseler; Roberta A Berard; Lori Broderick; Fatma Dedeoglu; Michelle Diebold; Karen Durrant; Polly Ferguson; Dirk Foell; Jonathan S Hausmann; Olcay Y Jones; Daniel Kastner; Helen J Lachmann; Ronald M Laxer; Dorelia Rivera; Nicola Ruperto; Anna Simon; Marinka Twilt; Joost Frenkel; Hal M Hoffman; Adriana A de Jesus; Jasmin B Kuemmerle-Deschner; Seza Ozen; Marco Gattorno; Raphaela Goldbach-Mansky; Erkan Demirkaya
Journal:  Arthritis Rheumatol       Date:  2022-05-27       Impact factor: 15.483

3.  Primary immunodeficiency diseases in different age groups: a report on 1,008 cases from a single Brazilian reference center.

Authors:  Magda Carneiro-Sampaio; Dewton Moraes-Vasconcelos; Cristina M Kokron; Cristina M A Jacob; Myrthes Toledo-Barros; Mayra B Dorna; Letícia A Watanabe; Ana Karolina B B Marinho; Ana Paula Moschione Castro; Antonio C Pastorino; Clóvis Artur A Silva; Maurício D Ferreira; Luiz V Rizzo; Jorge E Kalil; Alberto J S Duarte
Journal:  J Clin Immunol       Date:  2013-01-29       Impact factor: 8.317

4.  CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature-a rare case with a novel mutation.

Authors:  Miria Paula V Cavalcante; Juliana B Brunelli; Clarissa C Miranda; Glaucia V Novak; Louise Malle; Nadia E Aikawa; Adriana A Jesus; Clovis Artur Silva
Journal:  Eur J Pediatr       Date:  2015-11-14       Impact factor: 3.183

Review 5.  NOD1 and NOD2 in inflammatory and infectious diseases.

Authors:  Bruno C Trindade; Grace Y Chen
Journal:  Immunol Rev       Date:  2020-07-17       Impact factor: 12.988

Review 6.  Revisiting TNF Receptor-Associated Periodic Syndrome (TRAPS): Current Perspectives.

Authors:  Cornelia Cudrici; Natalie Deuitch; Ivona Aksentijevich
Journal:  Int J Mol Sci       Date:  2020-05-05       Impact factor: 5.923

7.  Computational Modeling of NLRP3 Identifies Enhanced ATP Binding and Multimerization in Cryopyrin-Associated Periodic Syndromes.

Authors:  Jenny Mae Samson; Dinoop Ravindran Menon; Prasanna K Vaddi; Nazanin Kalani Williams; Joanne Domenico; Zili Zhai; Donald S Backos; Mayumi Fujita
Journal:  Front Immunol       Date:  2020-11-19       Impact factor: 7.561

8.  An autoinflammatory syndrome with compound heterozygous MEFV and NOD2/CARD15 gene mutations successfully treated with tocilizumab.

Authors:  Jeanie Lee; Lilian Bizzocchi; Ruchi Jain; Clement E Tagoe
Journal:  Rheumatol Adv Pract       Date:  2022-05-09

Review 9.  Autoinflammatory granulomatous diseases: from Blau syndrome and early-onset sarcoidosis to NOD2-mediated disease and Crohn's disease.

Authors:  Francesco Caso; Paola Galozzi; Luisa Costa; Paolo Sfriso; Luca Cantarini; Leonardo Punzi
Journal:  RMD Open       Date:  2015-07-20

Review 10.  Natural history of mevalonate kinase deficiency: a literature review.

Authors:  Shumin Zhang
Journal:  Pediatr Rheumatol Online J       Date:  2016-05-04       Impact factor: 3.054

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.